Rapid nitrosamine formation from a tertiary amine: The nitrosation of 2-(N,N-Dimethylaminomethyl)pyrrole

Autor:	J.R. Outram, J.M. Faulconer, Richard N. Loeppky, W. Tomasik
Rok vydání:	1983
Předmět:	Nitrous acid chemistry.chemical_compound chemistry Tertiary amine Nitrosamine Organic Chemistry Drug Discovery Nitrosation Formaldehyde Organic chemistry Biochemistry Pyrrole
Zdroj:	Tetrahedron Letters. 24:4271-4274
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(00)88318-5
Popis:	2-(N,N-Dimethylaminomethyl)pyrrole reacts instantaneously with nitrous acid at 25° to produce diemthylnitrosamine, maleimidemonooxine, formaldehyde and other products. The data implicate new mechanisms of tertiary amine nitrosation.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::5e228a6fcfd2bc6a98de48e665efa99f https://doi.org/10.1016/s0040-4039(00)88318-5 Zobrazit plný text záznamu